This submission belongs to the session e. Symposium on Microwave Assisted Synthesis of the event The 8th International Electronic Conference on Synthetic Organic Chemistry
Published date
01 Nov, 2004
Citation
Biswanath Das, G. Mahender, K. V.N.S. Srinivas, P. Madhusudhan, Microwave Prompted Transformations of Natural Antitumor Alkaloid 20-O-Acetyl-9-Methoxy Campothecin to Its Decarboxylated E-Ring Anologues1, in Proceedings of The 8th International Electronic Conference on Synthetic Organic Chemistry, 1 November–30 November 2004, MDPI: Basel, Switzerland, doi: 10.3390/ecsoc-8-01984
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Microwave Prompted Transformations of Natural Antitumor Alkaloid 20-O-Acetyl-9-Methoxy Campothecin to Its Decarboxylated E-Ring Anologues1
Biswanath Das 1
G. Mahender 1
K. V.N.S. Srinivas 1
P. Madhusudhan 1
1. Indian Institute of Chemical Technology, Hyderabad-500007, India
Abstract
Keywords
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Synthesis of N-Lupinylamines
Solvent-Free, Efficient Synthesis of 2,5-piperazinediones from BOC-Protected Dipeptides under Microwave Irradiation